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- W2078604670 abstract "Nuclear magnetic resonance (1H) at room and elevated temperatures has been used to study the tautomerism of a number of naphtho- and quinolino-furoxans. Free-energy differences between tautomers are, in general, small, while the activation energies for their equilibrations (ca. 20 kcal./mole) are ca. 6 kcal./mole higher than those of benzofuroxans. An attempt to prepare naphtho[2,3-c]furoxan was unsuccessful." @default.
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- W2078604670 date "1968-01-01" @default.
- W2078604670 modified "2023-10-14" @default.
- W2078604670 title "N-oxides and related compounds. Part XXXIV. The tautomerism of some naphtho-and quinolino-furoxans" @default.
- W2078604670 doi "https://doi.org/10.1039/j29680001516" @default.
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